List of variants in gene NCF4 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.758+51G>A	rs150640467	0.00021
NM_000631.5(NCF4):c.50C>T (p.Pro17Leu)	rs147322774	0.00019
NM_000631.5(NCF4):c.173G>A (p.Arg58His)	rs763314327	0.00003

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